FDA.reportPublic FDA data

ANTI-BACTERIAL HAND SANITIZER

Manufacturer
Dongguan Benoy Industrial CO.,LTD
Effective date
2020-05-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:29:33

Label at a glance#

ProductANTI-BACTERIAL HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Pump as needed into our palms and thoroughly spread on both hands. Rub into skin until dry

Storage and handling

Do not store in temperature over 118F

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria on the skin when water, soap &u to we are not available Recommend for repeated use

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

Do not apply around eyes Do not use in ears or mouth

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. In case of contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use or ask for a doctor if redness or irritation develops and persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

Pump as needed into our palms and thoroughly spread on both hands. Rub into skin until dry

Other information

STORAGE AND HANDLING SECTION

Do not store in temperature over 118F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin Propylene glycol Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75387-50175387-501-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER 934Z135WT9208IACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b963d83b-584e-c447-e053-2995a90ad973a60c5ff5-b8f4-1f0b-e053-2995a90a67a32021-01-21WarningsExact identifier
spl set id: a60c5ff5-b8f4-1f0b-e053-2995a90a67a3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.